Results 161 to 170 of about 52,401 (267)

A New Model of Feeding Biomechanics Based on Tied‐Arch Principles

open access: yesIntegrative Zoology, EarlyView.
This new biomechanical model explains the major stress and strain patterns generated through the cranium during biting. The model proposes that the cranium resolves bite‐induced reaction forces through arcs of compressive stress that span the cranial structure between biting teeth and both jaw joints.
D. Rex Mitchell
wiley   +1 more source

Oral Melanoma: A South American Collaborative Series of 21 Cases. [PDF]

open access: yesHead Neck Pathol
de Arruda JAA   +15 more
europepmc   +1 more source

Congenital Insufficiency of Soft Palate [PDF]

open access: yesProceedings of the Royal Society of Medicine, 1911
openaire   +2 more sources

Is Cone‐Beam CT Reliable for Apical Foramen Assessment? A Micro‐CT–Referenced Study

open access: yesAustralian Endodontic Journal, EarlyView.
ABSTRACT This study evaluated the diagnostic accuracy of two cone‐beam CT (CBCT) dose protocols for identifying the number and trajectory deviation of apical foramina. Forty lower molars were scanned in Micro‐CT. Thereafter, all teeth were inserted into the mandible sockets and a titanium implant and an endodontically treated tooth with a cobalt ...
João Pedro de Lima   +3 more
wiley   +1 more source

Persistent Wnt/β-catenin signaling disables soft palatogenesis and palatal osteogenesis by inducing mesenchymal condensation. [PDF]

open access: yesFront Cell Dev Biol
Wang B   +9 more
europepmc   +1 more source

Surgical Management of Non‐Allergic Rhinitis—An EAACI Task Force Position Paper

open access: yesAllergy, EarlyView.
ABSTRACT Non‐allergic rhinitis is a frequent yet underdiagnosed cause of chronic nasal symptoms, including nasal congestion, rhinorrhoea, and upper airway hyperreactivity. Its pathophysiology involves neurogenic dysregulation, leading to excessive mucus production and vasodilation.
Marie Lundberg   +18 more
wiley   +1 more source

Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature

open access: yesClinical Genetics, EarlyView.
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi   +6 more
wiley   +1 more source

Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval

open access: yesClinical Genetics, EarlyView.
This study reports a female proband with a de novo 9q34.11 deletion affecting SET, who underwent a 28‐year diagnostic odyssey after an atypical Rett syndrome clinical diagnosis. Genomic and proteomics analyses confirmed SET haploinsufficiency, refining the critical 9q34.11 region, and supporting speech therapy benefits in improving meaningful ...
Angelo Condell   +14 more
wiley   +1 more source

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